Canonical Allele Identifier: PA165842
Gene: RAD51D HGNC NCBI

Linked Data

ClinVar Variation Id: 141578
ClinVar RCV Id: RCV000130161 RCV000225779 RCV000238834 RCV001030594 RCV001284344 RCV001798441 RCV003952682
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002869.3:p.Val66Met
CA165840
NM_002878.4:c.196G>A